ClearanceBrief
510(k) K871697 ยท DXK Echocardiograph

GENESIS II

ApplicantBiosound, Inc., Indianapolis IN, US
DecisionSubstantially Equivalent, Nov 6, 1987
ReceivedApr 30, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K871697

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.